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Using Flow Cytometry to Screen Patients for X-linked Lymphoproliferative Disease Due to SAP Deficiency and XIAP Deficiency

X-linked lymphoproliferative disease is a rare congenital immunodeficiency that is most often caused by mutations in SH2D1A, the gene encoding signaling lymphocyte activation molecule (SLAM)-associated protein (SAP). XLP caused by SAP deficiency is most often characterized by fulminant mononucleosis...

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Detaylı Bibliyografya
Asıl Yazarlar: Marsh, Rebecca A., Bleesing, Jack J., Filipovich, Alexandra H.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2964414/
https://ncbi.nlm.nih.gov/pubmed/20816973
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jim.2010.08.010
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